Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia
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| Veröffentlicht in: | Clinical genetics 2014-11, Vol.86 (5), p.500-501 |
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| container_issue | 5 |
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| container_title | Clinical genetics |
| container_volume | 86 |
| creator | Wakil, S.M. Monies, D.M. Ramzan, K. Hagos, S. Bastaki, L. Meyer, B.F. Bohlega, S. |
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| doi_str_mv | 10.1111/cge.12312 |
| format | Article |
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| identifier | ISSN: 0009-9163 |
| ispartof | Clinical genetics, 2014-11, Vol.86 (5), p.500-501 |
| issn | 0009-9163 1399-0004 |
| language | eng |
| recordid | cdi_proquest_journals_1612682365 |
| source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
| subjects | Adolescent Adult Aged Base Sequence Child Child, Preschool DNA Mutational Analysis Exome - genetics Family Homozygote Humans Middle Aged Molecular Sequence Data Mutation - genetics N-Acetylgalactosaminyltransferases - genetics Spastic Paraplegia, Hereditary - genetics |
| title | Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia |
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